Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs11681792 1.000 0.080 2 49957256 intron variant C/T snv 0.12 4
rs3743832 1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4